Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu
Trial record 2 of 38 for:    cemiplimab

Study Evaluating Cemiplimab Alone and Combined With RP1 in Treating Advanced Squamous Skin Cancer (CERPASS)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04050436
Recruitment Status : Recruiting
First Posted : August 8, 2019
Last Update Posted : September 11, 2019
Sponsor:
Collaborator:
Regeneron Pharmaceuticals
Information provided by (Responsible Party):
Replimune Inc.

Brief Summary:
To estimate the clinical benefit of cemiplimab monotherapy versus cemiplimab in combination with RP1 for patients with locally advanced or metastatic CSCC, as assessed by overall response rate (ORR) according to central review.

Condition or disease Intervention/treatment Phase
Cutaneous Squamous Cell Carcinoma Advanced Cutaneous Squamous Cell Carcinoma Metastatic Cutaneous Squamous Cell Carcinoma Drug: Cemiplimab Biological: RP1 Phase 2

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 240 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Randomized, Controlled, Open-Label, Phase 2 Study of Cemiplimab as a Single Agent and in Combination With RP1 in Patients With Advanced Cutaneous Squamous Cell Carcinoma
Estimated Study Start Date : September 2019
Estimated Primary Completion Date : October 2022
Estimated Study Completion Date : March 2024

Arm Intervention/treatment
Experimental: Cemiplimab in combination with RP1
Cemiplimab administered intravenously every 3 weeks in combination with RP1 administered as an intratumoral injection every 3 weeks
Drug: Cemiplimab
Cemiplimab administered intravenously
Other Name: Libtayo

Biological: RP1
RP1 administered intratumorally
Other Name: Genetically modified herpes simplex type 1 virus

Active Comparator: Cemiplimab
Cemiplimab administered intravenously as a single therapy every 3 weeks
Drug: Cemiplimab
Cemiplimab administered intravenously
Other Name: Libtayo




Primary Outcome Measures :
  1. Objective Response Rate (ORR) based on Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 according to central review [ Time Frame: 36 months ]

Secondary Outcome Measures :
  1. ORR for patients with metastatic or locally advanced disease [ Time Frame: 36 months ]
  2. ORR for patients who have and have not previously received systemic CSCC-directed therapy [ Time Frame: 36 months ]
  3. ORR by investigator assessment [ Time Frame: approximately 36 months ]
  4. Rate of individual tumor response in injected versus non-injected lesions [ Time Frame: 36 months ]
  5. Duration of Response (DOR) per central and investigator review [ Time Frame: 36 months ]
  6. Progression-free Survival (PFS) per central and investigator review [ Time Frame: 36 months ]
  7. Complete response (CR) rate per central and investigator review [ Time Frame: 36 months ]
  8. Overall Survival (OS) [ Time Frame: approximately 36 months ]
  9. Evaluation of the safety and tolerability of cemiplimab alone and combined with RP1 as assessed via adverse events (AEs) [ Time Frame: 36 months ]
    Overall adverse event rates and adverse event rates per observation period will be compared for the two treatment groups using a two-sided Fisher Exact test. Results will be analyzed by SOC and for preferred terms with >10% overall incidence.

  10. Change in overall scores of patient-reported outcomes in European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30) [ Time Frame: 36 months ]


Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Key Inclusion Criteria:

  • Histologically confirmed locally advanced or metastatic cutaneous squamous cell carcinoma
  • Patients for whom surgical or radiological treatment of lesions is contraindicated
  • At least 1 lesion that is measurable and injectable by study criteria (tumor of ≥1cm in longest diameter or ≥1.5 cm in shortest diameter for lymph nodes).
  • Eastern Cooperative Oncology Group (ECOG) performance status ≤1
  • Anticipated life expectancy >12 weeks
  • All patients must consent to provide archived or newly obtained tumor material for central pathology review for confirmation of diagnosis of CSCC.

Key Exclusion Criteria:

  • Prior treatment with an oncolytic therapy
  • Patients with active significant herpetic infections or prior complications of HSV-1 infection (e.g. herpetic keratitis or encephalitis)
  • Patients who require intermittent or chronic use of systemic (oral or intravenous) anti-virals with known anti-herpetic activity (e.g. acyclovir)
  • Ongoing or recent (within 5 years) evidence of significant autoimmune disease that required treatment with systemic immunosuppressive treatments
  • Prior treatment with an agent that blocks the PD-1/PD-L1 pathway.
  • Prior treatment with other immune modulating agents other than as adjuvant or neoadjuvant therapy.
  • Untreated brain metastasis(es) that may be considered active.
  • Known infection including active infection with hepatitis B virus (HBV), hepatitis C virus (HCV) or human immunodeficiency virus (HIV).
  • History of ILD/pneumonitis within the last 5 years or a history of ILD/pneumonitis requiring treatment with systemic steroids.

Note: Other protocol defined Inclusion/Exclusion criteria apply.


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04050436


Contacts
Layout table for location contacts
Contact: CERPASS Study +1 (781) 995-2443 CERPASS@replimune.com

Locations
Layout table for location information
Australia, Queensland
Tasman Oncology Research Ltd Recruiting
Southport, Queensland, Australia
Contact: Andrew Hill, MD         
Sponsors and Collaborators
Replimune Inc.
Regeneron Pharmaceuticals
Investigators
Layout table for investigator information
Study Director: Howard Kaufman, MD Chief Medical Officer

Layout table for additonal information
Responsible Party: Replimune Inc.
ClinicalTrials.gov Identifier: NCT04050436     History of Changes
Other Study ID Numbers: RPL-002-18
First Posted: August 8, 2019    Key Record Dates
Last Update Posted: September 11, 2019
Last Verified: September 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

Layout table for additional information
Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Replimune Inc.:
Oncolytic Virus
Carcinoma
Carcinoma, Squamous Cell
Cemiplimab
Metastatic Cutaneous Squamous Cell Carcinoma
Oncolytic Immuno-gene therapy
Additional relevant MeSH terms:
Layout table for MeSH terms
Carcinoma
Carcinoma, Squamous Cell
Neoplasms, Glandular and Epithelial
Neoplasms by Histologic Type
Neoplasms
Neoplasms, Squamous Cell